510(k) Report

FDA applicant

Laboratory Data Control

Mchenry, IL4 decisions1980–19800 recalls

FDA records 4 decisions for Laboratory Data Control (Mchenry, IL) in 1980: 4 510(k) clearances. All are in product code KIE (Apparatus, High Pressure Liquid Chromatography). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Laboratory Data Control’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laboratory Data Control since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Laboratory Data Control by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KIEApparatus, High Pressure Liquid Chromatography4decisions

What has FDA decided for it lately?

  • K800289LDC Spectromonitor IiiLaboratory Data Control · 1980
  • K800046LDC Chromatography Accessory Module BLaboratory Data Control · 1980
  • K800048LDC Constametric Iii Hight Press. Sol.Laboratory Data Control · 1980
  • K800047LDC Uviii Fixed Wavelength UltravioletLaboratory Data Control · 1980

All 4 as Laboratory Data Control →